Team:TUDelft/24 August 2009

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24 August 2009

Sriram

Today I did the restriction of all the DNA I minipreped on friday. The gel image below shows the restricted samples.

Gel240809-Delay Assembly1-8.jpg

Then I also ligated and transformed the assemblies for riboregulator and stopped the negative cascade assembly since Daniel's backup plan for it progressing very well.

Daniel

Transformaltion of friday 21-08-2009 looked good. On each plate there were 80-90 colonies

Digestion of assemblies in order to do the second round of assembly. Gel 1% (left) for Calin´s PCR and 2% (right) for my digestions and Calin´s PCR

Gel240809.jpg


Left Gel (2%)

Well Assembly Expected Plasmid Size Status
1 [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder]
2 col PCR 1 1616
3 col PCR 2 1616
4 col PCR 3 1616
5 col PCR 4 1616
6 col PCR 5 1616
7 col PCR 6 1616
8 [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder]

Right Gel (1%)

Well Assembly Expected Plasmid Size Status
1 [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder]
2 4A 824  ?
3 5A 1040
4 2A 214  ?
5 3A 183  ?
6 1A 1076  ?
7 col PCR 1 1616
8 col PCR 2 1616
9 col PCR 3 1616
10 col PCR 4 1616
11 col PCR 5 1616
12 col PCR 6 1616

Prepare IPTG 1M for further induction. I tried to do an experiment with 1A which is GFP under control of PLacI however the culture glows even though there is no IPTG induction.

We got the oligo for the two locks and keys I designed.